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Co-Reactivation of Cytomegalovirus and Epstein-Barr Virus Was Associated With Poor Prognosis After Allogeneic Stem Cell Transplantation

Reactivation of cytomegalovirus (CMV) or Epstein-Barr virus (EBV) is common after hematopoietic stem cell transplantation (HSCT). Previous researches have demonstrated that either CMV or EBV reactivation is associated with poor outcomes of HSCT. However, few studies investigate the impact of CMV and...

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Autores principales: Zhou, Jing-Rui, Shi, Da-Yu, Wei, Rong, Wang, Yu, Yan, Chen-Hua, Zhang, Xiao-Hui, Xu, Lan-Ping, Liu, Kai-Yan, Huang, Xiao-Jun, Sun, Yu-Qian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7921792/
https://www.ncbi.nlm.nih.gov/pubmed/33664733
http://dx.doi.org/10.3389/fimmu.2020.620891
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author Zhou, Jing-Rui
Shi, Da-Yu
Wei, Rong
Wang, Yu
Yan, Chen-Hua
Zhang, Xiao-Hui
Xu, Lan-Ping
Liu, Kai-Yan
Huang, Xiao-Jun
Sun, Yu-Qian
author_facet Zhou, Jing-Rui
Shi, Da-Yu
Wei, Rong
Wang, Yu
Yan, Chen-Hua
Zhang, Xiao-Hui
Xu, Lan-Ping
Liu, Kai-Yan
Huang, Xiao-Jun
Sun, Yu-Qian
author_sort Zhou, Jing-Rui
collection PubMed
description Reactivation of cytomegalovirus (CMV) or Epstein-Barr virus (EBV) is common after hematopoietic stem cell transplantation (HSCT). Previous researches have demonstrated that either CMV or EBV reactivation is associated with poor outcomes of HSCT. However, few studies investigate the impact of CMV and EBV co-reactivation after HSCT. In this study, we described the clinical characteristics of HSCT recipients with CMV and EBV co-reactivation (defined as CMV and EBV viremia occur at the same period of time). We conducted a longitudinal study of 247 patients who underwent HSCT in our center. A total of 24 (9.7%) patients had CMV and EBV co-reactivation. These patients showed higher incidence of viral pneumonitis (P=0.005). Patients with CMV and EBV co-reactivation had significant lower 1-year overall survival (OS) (P=0.004) and lower 1-year leukemia free survival (LFS) (P=0.016). Our further analysis suggested that duration of CMV (P=0.014), EBV (P<0.001), and CD4+CD25+ T cell counts at day 30 post-transplantation (P=0.05) are independent risk factors of virus co-reactivation. In conclusion, patients who developed co-reactivation of CMV and EBV had poor prognosis in terms of lower 1-year OS and LFS, and the CMV and EBV co-reactivation was associated with prolonged CMV or EBV duration and poor CD4+CD25+ T cell reconstitution at day 30 post-transplantation.
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spelling pubmed-79217922021-03-03 Co-Reactivation of Cytomegalovirus and Epstein-Barr Virus Was Associated With Poor Prognosis After Allogeneic Stem Cell Transplantation Zhou, Jing-Rui Shi, Da-Yu Wei, Rong Wang, Yu Yan, Chen-Hua Zhang, Xiao-Hui Xu, Lan-Ping Liu, Kai-Yan Huang, Xiao-Jun Sun, Yu-Qian Front Immunol Immunology Reactivation of cytomegalovirus (CMV) or Epstein-Barr virus (EBV) is common after hematopoietic stem cell transplantation (HSCT). Previous researches have demonstrated that either CMV or EBV reactivation is associated with poor outcomes of HSCT. However, few studies investigate the impact of CMV and EBV co-reactivation after HSCT. In this study, we described the clinical characteristics of HSCT recipients with CMV and EBV co-reactivation (defined as CMV and EBV viremia occur at the same period of time). We conducted a longitudinal study of 247 patients who underwent HSCT in our center. A total of 24 (9.7%) patients had CMV and EBV co-reactivation. These patients showed higher incidence of viral pneumonitis (P=0.005). Patients with CMV and EBV co-reactivation had significant lower 1-year overall survival (OS) (P=0.004) and lower 1-year leukemia free survival (LFS) (P=0.016). Our further analysis suggested that duration of CMV (P=0.014), EBV (P<0.001), and CD4+CD25+ T cell counts at day 30 post-transplantation (P=0.05) are independent risk factors of virus co-reactivation. In conclusion, patients who developed co-reactivation of CMV and EBV had poor prognosis in terms of lower 1-year OS and LFS, and the CMV and EBV co-reactivation was associated with prolonged CMV or EBV duration and poor CD4+CD25+ T cell reconstitution at day 30 post-transplantation. Frontiers Media S.A. 2021-02-16 /pmc/articles/PMC7921792/ /pubmed/33664733 http://dx.doi.org/10.3389/fimmu.2020.620891 Text en Copyright © 2021 Zhou, Shi, Wei, Wang, Yan, Zhang, Xu, Liu, Huang and Sun http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Zhou, Jing-Rui
Shi, Da-Yu
Wei, Rong
Wang, Yu
Yan, Chen-Hua
Zhang, Xiao-Hui
Xu, Lan-Ping
Liu, Kai-Yan
Huang, Xiao-Jun
Sun, Yu-Qian
Co-Reactivation of Cytomegalovirus and Epstein-Barr Virus Was Associated With Poor Prognosis After Allogeneic Stem Cell Transplantation
title Co-Reactivation of Cytomegalovirus and Epstein-Barr Virus Was Associated With Poor Prognosis After Allogeneic Stem Cell Transplantation
title_full Co-Reactivation of Cytomegalovirus and Epstein-Barr Virus Was Associated With Poor Prognosis After Allogeneic Stem Cell Transplantation
title_fullStr Co-Reactivation of Cytomegalovirus and Epstein-Barr Virus Was Associated With Poor Prognosis After Allogeneic Stem Cell Transplantation
title_full_unstemmed Co-Reactivation of Cytomegalovirus and Epstein-Barr Virus Was Associated With Poor Prognosis After Allogeneic Stem Cell Transplantation
title_short Co-Reactivation of Cytomegalovirus and Epstein-Barr Virus Was Associated With Poor Prognosis After Allogeneic Stem Cell Transplantation
title_sort co-reactivation of cytomegalovirus and epstein-barr virus was associated with poor prognosis after allogeneic stem cell transplantation
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7921792/
https://www.ncbi.nlm.nih.gov/pubmed/33664733
http://dx.doi.org/10.3389/fimmu.2020.620891
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